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L-Leucinamide, N-[(phenylmethoxy)carbonyl]-L-leucyl-N-[3-fluoro-1-[[4-[(fluoroacetyl)oxy] phenyl]methyl]-2-oxopropyl]-, (R)is a complex organic compound derived from the amino acid leucine. It features a phenylmethoxy carbonyl group, a fluorine-substituted phenyl ring, and an oxopropyl group. The (R)designation indicates that the compound exhibits chirality, which may contribute to its unique properties and potential applications.

137362-98-2

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137362-98-2 Usage

Uses

Used in Pharmaceutical Industry:
L-Leucinamide, N-[(phenylmethoxy)carbonyl]-L-leucyl-N-[3-fluoro-1-[[4-[(fluoroacetyl)oxy] phenyl]methyl]-2-oxopropyl]-, (R)is used as a pharmaceutical compound for its potential therapeutic effects. The unique structural features and functional groups of L-Leucinamide, N-[(phenylmethoxy)carbonyl]-L-leucyl-N-[3-fluoro-1-[[4-[(fluoroacetyl)oxy] phenyl]methyl]-2-oxopropyl]-, (R)- may contribute to its ability to target specific biological pathways or interact with certain receptors, making it a promising candidate for the development of new drugs.
Used in Biotechnological Applications:
In the biotechnology field, L-Leucinamide, N-[(phenylmethoxy)carbonyl]-L-leucyl-N-[3-fluoro-1-[[4-[(fluoroacetyl)oxy] phenyl]methyl]-2-oxopropyl]-, (R)may be utilized for various purposes, such as enzyme inhibition, protein modification, or as a building block for the synthesis of more complex molecules. Its chirality and functional groups can provide specific interactions with biological systems, making it a valuable tool for research and development in biotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 137362-98-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,3,6 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 137362-98:
(8*1)+(7*3)+(6*7)+(5*3)+(4*6)+(3*2)+(2*9)+(1*8)=142
142 % 10 = 2
So 137362-98-2 is a valid CAS Registry Number.

137362-98-2Relevant academic research and scientific papers

Inactivation of calpain by peptidyl fluoromethyl ketones

Angliker,Anagli,Shaw

, p. 216 - 220 (2007/10/02)

The syntheses of Z-Leu-Leu-Tyr-CH2F (1) and Z-Tyr-Ala-CH2F (3) are described. The ability of Z-Leu-Leu-Tyr-CH2F (1) and Z-Leu-Tyr-CH2F (2) to inactivate in vitro calcium-activated proteinase from chicken gizzard

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